ClinVar Miner

Submissions for variant NM_005026.5(PIK3CD):c.321C>T (p.Asp107=)

gnomAD frequency: 0.00001  dbSNP: rs1017772805
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002167264 SCV002338857 likely benign Immunodeficiency 14 2021-07-14 criteria provided, single submitter clinical testing

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